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Description
3-Methyl-4-nitroquinoline 1-Oxide is a heterocyclic chemical compound that serves as a building block in organic synthesis within the chemistry laboratory. It is a quinoline derivative carrying a methyl group at position three, a nitro group at position four, and an N-oxide group on the ring nitrogen atom. The simultaneous presence of several functional groups makes it a highly valuable intermediate for assembling more complex molecules, such as bioactive compounds, dyes, metal ligands, and pharmaceutical candidates. In the laboratory, this product is generally used as a starting material or reaction intermediate for constructing quinoline frameworks that are widely found in active compounds, and it therefore functions as a research chemical that supports the development of new substances.
As a research chemical, this product supports the development of new compounds, and its main advantage lies in a structure that is rich in functional groups, offering many reaction sites for the synthesis designer. The N-oxide group provides distinctive reactivity that enables selective chemical transformations, while the nitro group can be reduced to an amine for the synthesis of new derivatives. This combination of features makes 3-Methyl-4-nitroquinoline 1-Oxide a preferred choice for researchers who need a versatile, multifunctional scaffold for heterocyclic chemistry and medicinal chemistry programs, since the multiple points of modification allow flexible route planning and broad structural exploration.
In Indonesian laboratories, this compound is typically employed as a research-grade starting material in organic synthesis work and in studies focused on heterocyclic chemistry. Researchers use it to prepare quinoline-based intermediates for bioactive molecule discovery, ligand design, and materials science experiments. As a product distributed by AMI Scientific under the TCI brand, it is supplied to academic institutions, research centers, and pharmaceutical development facilities that require reliable building blocks for constructing new molecular structures and for exploring structure-activity relationships.
Laboratory Applications
- Organic synthesis of quinoline derivatives: The compound's methyl, nitro, and N-oxide groups provide multiple reactive sites for building substituted quinoline frameworks in multi-step synthetic routes.
- Preparation of amines via nitro reduction: The nitro group at position four can be selectively reduced to an amine, enabling access to aminoquinoline intermediates for further derivatization.
- Medicinal chemistry research: As a multifunctional scaffold, it supports the assembly of bioactive molecules and pharmaceutical candidate structures that incorporate quinoline cores.
- Ligand and coordination chemistry: The N-oxide and nitro functionalities can participate in metal coordination, making the compound useful for preparing metal ligands and coordination complexes.
- Dye and specialty chemical development: Its electron-rich and electron-poor functional groups allow controlled modification toward chromophore structures used in dye and specialty chemical research.
Specifications
- Brand: TCI
- Catalog number: M3311
- CAS number: 14073-00-8
- Category: Chemistry > Building Blocks > Heterocyclic Building Blocks
- Physical form: Not specified in the available product data
- Pack sizes: Not specified in the available product data
- Storage note: Store in a cool, dry, well-ventilated area, protected from light and heat
Handling and Storage
Store the product in its original, tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Keep it separated from strong oxidizing agents and incompatible reactive materials. Always use appropriate personal protective equipment, including a laboratory coat, safety goggles, and chemical-resistant gloves, when handling the compound. Work inside a fume hood to avoid inhaling dust or vapors, and avoid any skin or eye contact. Wash hands thoroughly after handling, keep the container clearly labeled, and follow standard laboratory procedures for the safe disposal of chemical residues.
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